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ENZYME REPLACEMENT THERAPY IN GAUCHER'S AND FABRY'S DISEASE.PENTCHEV PG.1977; ANN. CLIN. LAB. SCI.; U.S.A.; DA. 1977; VOL. 7; NO 3; PP. 251-253; BIBL. 5 REF.Article

THE EFFECT OF A HEAST-STABLE FACTOR IN HUMAN SPLEEN ON GLUCOCEREBROSIDASE AND ACID BETA -GLUCOSIDASE ACTIVITIESPENTCHEV PG; BRADY RO.1973; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1973; VOL. 297; NO 2; PP. 491-496; BIBL. 7REF.Serial Issue

INVESTIGATIONS IN ENZYME REPLACEMENT THERAPY IN LIPID STORAGE DISEASESBRADY RO; PENTCHEV PG; GAL AE et al.1975; FEDER. PROC.; U.S.A.; DA. 1975; VOL. 34; NO 5; PP. 1310-1315; BIBL. 35REF.Serial Issue

EVOLUTION OF ENZYME REPLACEMENT THERAPY FOR LIPID STORAGE DISEASES = EVOLUTION DU TRAITEMENT DES LIPIDOSES PAR REMPLACEMENT DES ENZYMESBRADY RO; GAL AE; PENTCHEV PG et al.1974; LIFE SCI.; G.B.; DA. 1974; VOL. 15; NO 7; PP. 1235-1248; BIBL. 2P.1/2Article

A NOVEL CHROMOGENIC SUBSTRATE FOR ASSAYING GLUCOCEREBROSIDASE ACTIVITY.GAL AE; PENTCHEV PG; FASH FJ et al.1976; PROC. SOC. EXPER. BIOL. MED.; U.S.A.; DA. 1976; VOL. 153; NO 2; PP. 363-366; BIBL. 10 REF.Article

AN ENZYMOLOGICAL APPROACH TO THE LIPIDOSESTALLMAN JF; PENTCHEV PG; BRADY RO et al.1974; ENZYME; SWITZ.; DA. 1974; VOL. 18; NO 12; PP. 136-149; BIBL. 4P.Article

STUDIES IN VIVO OF THE TISSUE UPTAKE, CELLULAR DISTRIBUTION AND CATABOLIC TURNOVER OF EXOGENOUS GLUCOCEREBROSIDASE IN RATMORRONE S; PENTCHEV PG; BAYNES J et al.1981; BIOCHEM. J. (LOND.); ISSN 0006-2936; GBR; DA. 1981; VOL. 194; NO 3; PP. 733-742; BIBL. 2 P.Article

THE DIAGNOSIS OF TYPE A AND TYPE B NIEMANN-PICK DISEASE AND DETECTION OF CARRIERS USING LEUKOCYTES AND A CHROMOGENIC ANALOGUE OF SPHINGOMYELINGAL AE; BRADY RO; BARRANGER JA et al.1980; CLIN. CHIM. ACTA; NLD; DA. 1980; VOL. 104; NO 1; PP. 129-132; BIBL. 16 REF.Article

REPLACEMENT THERAPY OF INHERITED ENZYME DEFIENCY. USE OF PURIFIED GLUCOCEREBROSIDASE IN GAUCHER'S DISEASE = THERAPEUTIQUE SUBSTITUTIVE DES DEFICIENCES ENZYMATIQUES HEREDITAIRES: UTILISATION DE LA GLUCOCEREBROSIDASE PURIFIEE DANS LA MALADIE DE GAUCHERBRADY RO; PENTCHEV PG; GAL AE et al.1974; NEW ENGL. J. MED.; U.S.A.; DA. 1974; VOL. 291; NO 19; PP. 989-993; BIBL. 22REF.Article

L-GLUCOSYLCERAMIDE: SYNTHESIS, PROPERTIES, AND RESISTANCE TO CATABOLISM BY GLUCOCEREBROSIDASE IN VITROGAL AF; PENTCHEV PG; MASSEY JM et al.1979; PROC. NATION. ACAD. SCI.; USA; DA. 1979; VOL. 76; NO 7; PP. 3083-3086; BIBL. 15 REF.Article

THE DISTRIBUTION OF GLUCOCEREBROSIDE IN THE LIVER OF PATIENTS WITH GAUCHER'S DISEASEGAL AE; PENTCHEV PG; BARRANGER JA et al.1979; ANAL BIOCHEM.; USA; DA. 1979; VOL. 95; NO 1; PP. 127-132; BIBL. 14 REF.Article

THE ISOLATION AND CHARACTERIZATION OF SPHINGOMYELINASE FROM HUMAN PLACENTAL TISSUE.PENTCHEV PG; BRADY RO; GAL AE et al.1977; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1977; VOL. 488; NO 2; PP. 312-321; BIBL. 25 REF.Article

GAUCHER DISEASE: ISOLATION AND COMPARISON OF NORMAL AND MUTANT GLUCOCERESIDASE FROM HUMAN SPLEEN TISSUEPENTCHEV PG; BRADY RO; BLAIR HE et al.1978; PROC. NATION. ACAD. SCI. USA; USA; DA. 1978; VOL. 75; NO 8; PP. 3970-3973; BIBL. 14 REF.Article

A NEW FORM OF NIEMANN-PICK DISEASE CHARACTERISED BY TEMPERATURE-LABILE SPHINGOMYELINASESCHNEIDER EL; PENTCHEV PG; HIBBERT SR et al.1978; J. MED. GENET.; GBR; DA. 1978; VOL. 15; NO 5; PP. 370-374; BIBL. 19 REF.Article

REPLACEMENT THERAPY FOR INHERITED ENZYME DEFICIENCY. SUSTAINED CLEARANCE OF ACCUMULATED GLUCOCEREBROSIDE IN GAUCHER'S DISEASE FOLLOWING INFUSION OF PURIFIED GLUCOCEREBROSIDASE. = TRAITEMENT DE SUBSTITUTION D'UN DEFICIT ENZYMATIQUE HEREDITAIRE; MAINTIEN DE LA CLEARANCE DU GLUCOCEREBROSIDE ACCUMULE DANS LA MALADIE DE GAUCHER APRES UNE INJECTION DE GLUCOCEREBROSIDASE PURIFIEEPENTCHEV PG; BRADY RO; GAL AE et al.1975; J. MOLEC. MED.; NETHERL.; DA. 1975; VOL. 1; NO 1; PP. 73-78; BIBL. 11 REF.Article

STUDIES OF LYSOSOMAL FUNCTION. I. METABOLISM OF SOME COMPLEX LIPIDS BY ISOLATED HEPATOCYTES AND KUPFFER CELLSBARRANGER JA; PENTCHEV PG; FURBISH FS et al.1978; BIOCHEM. BIOPHYS. RES. COMMUNIC.; USA; DA. 1978; VOL. 83; NO 3; PP. 1055-1060; BIBL. 28 REF.Article

PATHOGENESIS OF ONE VARIANT OF SEA-BLUE HISTIOCYTOSIS = PATHOGENESE D'UN TYPE D'HISTIOCYTOSE "SEA-BLEU"GOLDE DW; SCHNEIDER EL; BAINTON DF et al.1975; LAB. INVEST.; U.S.A.; DA. 1975; VOL. 33; NO 4; PP. 371-378; BIBL. 32 REF.Article

MODIFICATION BY THE BLOOD-BRAIN BARRIER: INCREASED CONCENTRATION AND FATE OF ENZYMES ENTERING THE BRAINBARRANGER JA; RAPOPORT SI; FREDERICKS WR et al.1979; PROC. NATION. ACAD. SCI. USA; USA; DA. 1979; VOL. 76; NO 1; PP. 481-485; BIBL. 29 REF.Article

NIEMANN-PICK DISEASE EXPERIMENTAL MODEL: SPHINGOMYELINASE REDUCTION INDUCED BY AY-9944.SAKURAGAWA N; SAKURAGAWA M; KUWABARA T et al.1977; SCIENCE; U.S.A.; DA. 1977; VOL. 196; NO 4287; PP. 317-319; BIBL. 14 REF.Article

BILIARY EXCRETION OF GLYCOLIPID IN INDUCED OR INHERITED GLUCOSYLCERAMIDE LIPIDOSISPENTCHEV PG; WONG R; GAL AE et al.1981; BIOCHIM. BIOPHYS. ACTA; ISSN 0006-3002; NLD; DA. 1981; VOL. 665; NO 3; PP. 615-618; BIBL. 12 REF.Article

A LYSOSOMAL STORAGE DISORDER IN MICE CHARACTERIZED BY A DUAL DEFICIENCY OF SPHINGOMYELINASE AND GLUCOCEREBROSIDASEPENTCHEV PG; GAL AE; BOOTH AD et al.1980; BIOCHIM. BIOPHYS. ACTA; ISSN 0006-3002; NLD; DA. 1980; VOL. 619; NO 3; PP. 669-679; BIBL. 26 REF.Article

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